Bhisey R A, Ramchandani A G, Veturkar P L, Borges A M, Notani P N, Sirsat S M
Genotoxicity Unit, Cancer Research Institute, Bombay, India.
J Cancer Res Clin Oncol. 1988;114(3):279-82. doi: 10.1007/BF00405834.
The effects of TPA, PDD, PDB, PDA, or MEZ on epithelial and mesenchymal skin tumors induced by a s.c. injection of MCA were studied histologically. Group-I mice received only MCA. At 6 weeks after MCA injection, mice in groups II to VII received acetone, 1.8 nmol TPA, PDD, PDB, PDA, or 6.1 nmol MEZ respectively in 0.1 ml acetone twice weekly until tumor development. Alterations in skin tumor induction patterns were also studied in animals that had been exposed to TPA or acetone for 10 weeks prior to s.c. injection of MCA. Exposure of mouse skin to TPA before or after carcinogen administration increased 2- to 3.5-fold, the incidence of carcinoma and mixed tumors of epithelial and mesenchymal histogenesis. The average time of tumor induction decreased in mice treated with MCA + TPA and 100% of the test animals in the TPA + MCA group developed tumors. In contrast, TPA-related phorbol esters inhibited skin tumor development, particularly trichoepithelioma and fibrosarcoma and increased the average time of tumor induction.
通过组织学方法研究了佛波醇-12,13-十四烷酸酯(TPA)、4β-佛波醇-12,13-十四烷酸酯(PDD)、4α-佛波醇-12,13-十四烷酸酯(PDB)、4α-佛波醇-12,13-癸二酸酯(PDA)或12-O-十四烷酰佛波醇-13-乙酸酯(MEZ)对皮下注射甲基胆蒽(MCA)诱导的上皮性和间质性皮肤肿瘤的影响。第一组小鼠仅接受MCA。在注射MCA后6周,第二至七组小鼠分别每周两次接受丙酮、1.8 nmol TPA、PDD、PDB、PDA或6.1 nmol MEZ,每次0.1 ml丙酮,直至肿瘤发生。还对在皮下注射MCA前已暴露于TPA或丙酮10周的动物的皮肤肿瘤诱导模式改变进行了研究。在给予致癌物之前或之后使小鼠皮肤暴露于TPA,可使上皮和间质性组织发生的癌和混合瘤的发生率增加2至3.5倍。用MCA + TPA处理的小鼠肿瘤诱导的平均时间缩短,并且TPA + MCA组中100%的试验动物发生肿瘤。相反,与TPA相关的佛波酯抑制皮肤肿瘤的发展,特别是毛发上皮瘤和纤维肉瘤,并延长肿瘤诱导的平均时间。